国际脑血管病杂志
國際腦血管病雜誌
국제뇌혈관병잡지
INTERNATIONAL JOURNAL OF CEREBROVASCULAR DISEASES
2009年
12期
913-917
,共5页
杨志秀%王建林%罗丽华%张晓敏%范云虎%张扬
楊誌秀%王建林%囉麗華%張曉敏%範雲虎%張颺
양지수%왕건림%라려화%장효민%범운호%장양
生长激素%脑出血%血清白蛋白%肠黏膜%大鼠
生長激素%腦齣血%血清白蛋白%腸黏膜%大鼠
생장격소%뇌출혈%혈청백단백%장점막%대서
目的 评价重组人生长激素(recombinant human growth hormom,rhGH)对脑出血大鼠血清白蛋白水平和小肠黏膜形态学的影响.方法 采用自体血注射法制作大鼠脑出血模型.56只SD大鼠分为假手术组(n=8),rhGH组(n=24;腹腔注射rhGH,1 U/kg,1次/d)和生理盐水对照组(n=24;腹腔注射等量生理盐水,1次/d),后两组均分别再分为术后1、7和14 d组(每组n=8).检测各组大鼠不同时问点血清白蛋白浓度,HE染色和图像分析观察小肠黏膜形态学改变.结果 脑出血各时间点,生理盐水对照组血清白蛋白水平均较假手术组显著降低(P均<0.01);rhGH组血清白蛋白水平随治疗进程逐渐增高,但仅在14 d时显著高于生理盐水对照组[(39.93±1.98)g,L对(37.93±1.57)g,L,P<0.01].脑出血后1 d和7 d时,rhGH组小肠绒毛高度和黏膜厚度与生理盐水对照组无显著差异,但14 d时显著增高(P<0.01).脑出血后1、7和14 d小肠绒毛面积进行性缩小,且rhGH组较生理盐水对照组随治疗进程进行性增高(P<0.01).脑出血后1 d和7 d.rhGH组肠腺深度较生理盐水对照组增高(P<0.01),但14 d时无显著差异;脑出血1 d,rhGH组组肠腺密度较生理盐水对照组显著增高(P<0.01),7 d时增高不显著,14 d时不仅不增反而稍有降低.结论 脑出血大鼠血清白蛋白水平较假手术组显著下降;脑出血可引起小肠黏膜损害.rhGH可提高脑出血大鼠血清白蛋白水平,不论在脑出血早期还是后期均可不同程度减轻小肠黏膜损伤,后期改善更为显著.rhGH对小肠黏膜损伤的改善程度与血清白蛋白水平的升高程度呈正相关.
目的 評價重組人生長激素(recombinant human growth hormom,rhGH)對腦齣血大鼠血清白蛋白水平和小腸黏膜形態學的影響.方法 採用自體血註射法製作大鼠腦齣血模型.56隻SD大鼠分為假手術組(n=8),rhGH組(n=24;腹腔註射rhGH,1 U/kg,1次/d)和生理鹽水對照組(n=24;腹腔註射等量生理鹽水,1次/d),後兩組均分彆再分為術後1、7和14 d組(每組n=8).檢測各組大鼠不同時問點血清白蛋白濃度,HE染色和圖像分析觀察小腸黏膜形態學改變.結果 腦齣血各時間點,生理鹽水對照組血清白蛋白水平均較假手術組顯著降低(P均<0.01);rhGH組血清白蛋白水平隨治療進程逐漸增高,但僅在14 d時顯著高于生理鹽水對照組[(39.93±1.98)g,L對(37.93±1.57)g,L,P<0.01].腦齣血後1 d和7 d時,rhGH組小腸絨毛高度和黏膜厚度與生理鹽水對照組無顯著差異,但14 d時顯著增高(P<0.01).腦齣血後1、7和14 d小腸絨毛麵積進行性縮小,且rhGH組較生理鹽水對照組隨治療進程進行性增高(P<0.01).腦齣血後1 d和7 d.rhGH組腸腺深度較生理鹽水對照組增高(P<0.01),但14 d時無顯著差異;腦齣血1 d,rhGH組組腸腺密度較生理鹽水對照組顯著增高(P<0.01),7 d時增高不顯著,14 d時不僅不增反而稍有降低.結論 腦齣血大鼠血清白蛋白水平較假手術組顯著下降;腦齣血可引起小腸黏膜損害.rhGH可提高腦齣血大鼠血清白蛋白水平,不論在腦齣血早期還是後期均可不同程度減輕小腸黏膜損傷,後期改善更為顯著.rhGH對小腸黏膜損傷的改善程度與血清白蛋白水平的升高程度呈正相關.
목적 평개중조인생장격소(recombinant human growth hormom,rhGH)대뇌출혈대서혈청백단백수평화소장점막형태학적영향.방법 채용자체혈주사법제작대서뇌출혈모형.56지SD대서분위가수술조(n=8),rhGH조(n=24;복강주사rhGH,1 U/kg,1차/d)화생리염수대조조(n=24;복강주사등량생리염수,1차/d),후량조균분별재분위술후1、7화14 d조(매조n=8).검측각조대서불동시문점혈청백단백농도,HE염색화도상분석관찰소장점막형태학개변.결과 뇌출혈각시간점,생리염수대조조혈청백단백수평균교가수술조현저강저(P균<0.01);rhGH조혈청백단백수평수치료진정축점증고,단부재14 d시현저고우생리염수대조조[(39.93±1.98)g,L대(37.93±1.57)g,L,P<0.01].뇌출혈후1 d화7 d시,rhGH조소장융모고도화점막후도여생리염수대조조무현저차이,단14 d시현저증고(P<0.01).뇌출혈후1、7화14 d소장융모면적진행성축소,차rhGH조교생리염수대조조수치료진정진행성증고(P<0.01).뇌출혈후1 d화7 d.rhGH조장선심도교생리염수대조조증고(P<0.01),단14 d시무현저차이;뇌출혈1 d,rhGH조조장선밀도교생리염수대조조현저증고(P<0.01),7 d시증고불현저,14 d시불부불증반이초유강저.결론 뇌출혈대서혈청백단백수평교가수술조현저하강;뇌출혈가인기소장점막손해.rhGH가제고뇌출혈대서혈청백단백수평,불론재뇌출혈조기환시후기균가불동정도감경소장점막손상,후기개선경위현저.rhGH대소장점막손상적개선정도여혈청백단백수평적승고정도정정상관.
Objecthe To equate the effects of recombinant human growth hormone (rhGH) on serum albumin lewis and intestinal mucosal morphology in rats with intracerebral hemorrhage. Methods A rat model of intracerebral hemorrhage was induced by autologous blood injection. Fifty-six SD rats were divided into sham-operation group (n =8), rhGH group (n =24; intraperitoneal injection of rhGH, 1 U/kg, once a day), and saline control group (n =24; intraperitoneal injection of equivalent normal saline, once a day). The rhGH and saline control groups were redivided into 1-, 7- and 14-day groups (n =8 in each group) after the procedure. The serum albumin concentration was detected at different time points in all groups. The changes of intestinal mucosal morphology were observed with Hematoxylin and Eosin (HE)staining and image analysis. Results Hie serum albumin lewis at all time points of intracerebral hemorrhage in the saline control group were all significantly lower than those in the sham-operation group (all P < 0. 01); The serum albumin level was increased gradually with the treatment process in the rhGH group, however, it was only significantly higher than the saline control group at day 14 (39.93 ±1.98 g/L νs. 37. 93 ±1.57 g/L) (P<0. 01). There were no significant differences between the rhGH group and the saline group in intestinal villus height and mucosal thickness at day 1 and 7 after intracerebral hemorrhage, however they were increased significantly at day 14 (P <0.01). The area of intestinal villi was reduced progressively at day 1, 7 and 14 after intracerebral hemorrhage, and with the treatment process the rhGH group was increased more progressively than the saline control group (P <0. 01). The depth of intestinal glands in the rhGH group was increased significantly than that in the saline control group (P <0. 01), but there was no significant difference at day 14; the density of glands in the rhGH group was significantly increased than that in the saline group at day 1 after intracerebral hemorrhage (P < 0. 01), and it was not increased significantly at day 7, however, it was not increased but decreased slightly at day 14. Conclusions The serum albumin level in rats with intracerebral hemorrhage was decreased significantly than that in the sham-operation group, and intracerebral hemorrhage could cause intestinal mucosal injury. rhGH increased the serum albumin level in rats with intracerebral hemorrhage. It might reduce intestinal mucosal injury to different degrees whether it was in the early or late intracerebral hemorrhage, and the late improvement was more significant. The improvement degree of rhGH on intestinal mucosal injury was positively correlated with the increased degrees of the serum albumin level.